Treatment of Glaucoma Using Laquinimod

ABSTRACT

The subject invention provides a method of treating a subject afflicted with glaucoma, suffering from retinal ganglion cell (RGC) loss or damage, or elevated intraocular pressure (IOP), or of reducing RGC loss or damage, or reducing IOP in a subject, comprising administering to the subject an amount of laquinimod effective to treat the subject, to reduce RGC loss or damage, or to reduce IOP in the subject. Provide also is a pharmaceutical composition, a package and a therapeutic package for treating a subject afflicted with glaucoma.

This application claims benefit of U.S. Provisional Application No.61/904,962, filed Nov. 15, 2013, the entire content of which is herebyincorporated by reference herein.

Throughout this application, various publications are referred to byfirst author and year of publication. Full citations for thesepublications are presented in a References section immediately beforethe claims. Disclosures of the documents and publications referred toherein are hereby incorporated in their entireties by reference intothis application.

BACKGROUND

Glaucoma is a group of ocular diseases characterized by progressivedamage to the eye at least partly due to elevated intraocular pressure(IOP) (Merck Manual of Diagnosis and Therapy (1999)). Additionally,glaucoma is characterized by retinal ganglion cell (RGC) death, axonloss and an excavated appearance of the optic nerve head (Alward 1998).Glaucoma can be diagnosed before vision loss occurs by visual fieldtesting and by ophthalmoscopic examination of the optic nerve to detect“cupping.” The mean IOP in normal adults is 15 to 16 mm Hg; the normalrange is 10 to 21 mm Hg. One form of management of glaucoma is based onlowering the IOP using topically applied medications (Coleman 1999).

Currently there are five major classes of medications that are used tolower the IOP: β-adrenergic antagonists, adrenergic agonists,parasympathomimetics, prostaglandin-like analogues and carbonicanhydrase inhibitors (Medeiros et al. 2002). Although most medicationsare applied topically to the eye, they can cause severe systemic sideeffects and adversely affect the quality of the patient's life. Ifadditional lowering of IOP is indicated or if medication fails tosufficiently lower the IOP, laser trabeculoplasty is usually the nextstep. If IOP is still not adequately controlled, incisional glaucomasurgery is indicated (Id). The lowering of IOP, despite significantlyreducing the extent of neuronal loss, does not ensure cessation of thedisease process, because the loss of RGCs may continue. Recent studiesof the association between IOP regulation and visual field loss aftermedical or surgical intervention showed that ongoing neuronal lossreflected in visual field tests can be diminished if the IOP is low.However, neuronal loss may continue to occur after reduction of IOP(Bakalash et al. 2002).

Glaucomatous optic neuropathy appears to result from specificpathophysiological changes and subsequent death of RGCs and their axons.The process of RGC death is thought to be biphasic: a primary injuryresponsible for initiation of damage followed by a slower, secondarydegeneration attributable to the hostile environment surrounding thedegenerating cells (Kipnis et al. 2000).

The molecular mechanism triggering RGC death has not been identified.Deprivation of neurotrophic factors, ischemia, chronic elevation ofglutamate and disorganized nitric oxide metabolism are suspected to bepossible mechanisms (Farkas et al. 2001). In addition, it is possiblethat the mechanisms leading to RGC death share common features withother types of neuronal injury, such as signaling by reactive oxygenspecies, depolarization of mitochondria, or induction oftranscriptionally regulated cell death (Weinreb et al. 1999).

Laquinimod

Laquinimod (LAQ) is a novel synthetic compound with high oralbioavailability which has been suggested as an oral formulation for thetreatment of Multiple Sclerosis (MS) (Polman, 2005; Sandberg-Wollheim,2005). Laquinimod and its sodium salt form are described, for example,in U.S. Pat. No. 6,077,851. The mechanism of action of laquinimod is notfully understood. Animal studies show it causes a Th1 (T helper 1 cell,which produces pro-inflammatory cytokines) to Th2 (T helper 2 cell,which produces anti-inflammatory cytokines) shift with ananti-inflammatory profile (Yang, 2004; Brück, 2011). Another studydemonstrated (mainly via the NFkB pathway) that laquinimod inducedsuppression of genes related to antigen presentation and correspondinginflammatory pathways (Gurevich, 2010). Other suggested potentialmechanisms of action include inhibition of leukocyte migration into theCNS, increase of axonal integrity, modulation of cytokine production,and increase in levels of brain-derived neurotrophic factor (BDNF)(Runström, 2006; Brück, 2011).

The effects of laquinimod on glaucoma have not previously been studied.

SUMMARY OF THE INVENTION

The subject invention provides a method of treating a subject afflictedwith glaucoma comprising administering to the subject an amount oflaquinimod effective to treat the subject.

The subject invention also provides a method of treating a subjectsuffering from retinal ganglion cell loss or retinal ganglion celldamage, or of reducing retinal ganglion cell loss or damage in asubject, comprising administering to the subject an amount of laquinimodeffective to reduce retinal ganglion cell loss or retinal ganglion celldamage in the subject.

The subject invention also provides a method of treating a subjectsuffering from elevated intraocular pressure, or of reducing intraocularpressure in a subject, comprising administering to the subject an amountof laquinimod effective to reduce intraocular pressure in the subject.

The subject invention also provides a package comprising a) apharmaceutical composition comprising an amount of laquinimod; and b)instruction for use of the pharmaceutical composition to treat a subjectafflicted with glaucoma.

The subject invention also provides a therapeutic package for dispensingto, or for use in dispensing to, a subject afflicted with glaucoma,which comprises a) one or more unit doses, each such unit dosecomprising an amount of laquinimod thereof, wherein the amount of saidlaquinimod in said unit dose is effective, upon administration to saidsubject, to treat the subject, and b) a finished pharmaceuticalcontainer therefor, said container containing said unit dose or unitdoses, said container further containing or comprising labelingdirecting the use of said package in the treatment of said subject.

The subject invention also provides a pharmaceutical composition and apackage as described herein for use in treating a subject afflicted withglaucoma.

The subject invention also provides a pharmaceutical composition in unitdosage form, useful in treating a subject afflicted with glaucoma, whichcomprises an amount of laquinimod; which amount of said laquinimod insaid composition is effective, upon administration to said subject ofone or more of said unit dosage forms of said composition, to treat thesubject.

The subject invention also provides a package comprising a) apharmaceutical composition as described herein; and b) instruction foruse of the pharmaceutical composition to treat a subject afflicted withglaucoma.

The subject invention also provides laquinimod for the manufacture of amedicament for use in treating a subject afflicted glaucoma.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1: Example 1: Mean ATOP (OHT minus Non-OHT) (mmHg).

FIG. 2: Example 1: % Fluoro-gold Labeled RGC Loss.

FIG. 3: Example 1: Mean Fluoro-gold Labeled RGC count per mm².

FIG. 4: Optic Nerve Injury Grade (1-5).

FIG. 5A: Example 1: Representative images of the retinas with FG—labeledRGC—Animal Number 48, Group 1, Left Eye.

FIG. 5B: Example 1: Representative images of the retinas with FG—labeledRGC—Animal Number 48, Group 1, Right Eye.

FIG. 5C: Example 1: Representative images of the retinas with FG—labeledRGC—Animal Number 59, Group 2, Left Eye.

FIG. 5D: Example 1: Representative images of the retinas with FG—labeledRGC—Animal Number 59, Group 2, Right Eye.

FIG. 5E: Example 1: Representative images of the retinas with FG—labeledRGC—Animal Number 22, Group 3, Left Eye.

FIG. 5F: Example 1: Representative images of the retinas with FG—labeledRGC—Animal Number 22, Group 3, Right Eye.

FIG. 5G: Example 1: Representative images of the retinas with FG—labeledRGC—Animal Number 31, Group 4, Left Eye.

FIG. 5H: Example 1: Representative images of the retinas with FG—labeledRGC—Animal Number 31, Group 4, Right Eye.

FIG. 5I: Example 1: Representative images of the retinas with FG—labeledRGC—Animal Number 35, Group 5, Left Eye.

FIG. 5J: Example 1: Representative images of the retinas with FG—labeledRGC—Animal Number 35, Group 5, Right Eye.

DETAILED DESCRIPTION OF THE INVENTION

The subject invention provides a method of treating a subject afflictedwith glaucoma comprising administering to the subject an amount oflaquinimod effective to treat the subject.

In one embodiment, the administration of laquinimod is effective toreduce or inhibit a symptom of the glaucoma in the subject. In anotherembodiment, the symptom is retinal ganglion cell damage, retinalganglion cell loss, or elevated intraocular pressure. In anotherembodiment, laquinimod is laquinimod sodium.

In one embodiment, the route of administration of laquinimod isintraocular, periocular, systemic or topical. In another embodiment,laquinimod is administered via oral administration. In anotherembodiment, laquinimod is administered via ocular administration. Inanother embodiment, laquinimod is administered in the form of anaerosol, an inhalable powder, an injectable, a liquid, a gel, a solid, acapsule or a tablet.

In an embodiment, the concentration of laquinimod in the liquid or gelis 5-100 mg/ml solution, 20-100 mg/ml solution, 10-15 mg/ml solution, or20-50 mg/ml solution. In another embodiment, laquinimod is administeredperiodically. In another embodiment, laquinimod is administered daily.In another embodiment, laquinimod is administered more often than oncedaily. In yet another embodiment, laquinimod is administered less oftenthan once daily.

In one embodiment, the amount laquinimod administered is at least 0.2mg/day and/or less than 0.6 mg/day. In another embodiment, the amountlaquinimod administered is 0.03-600 mg/day, 0.1-40.0 mg/day, 0.1-2.5mg/day, 0.25-2.0 mg/day or 0.5-1.2 mg/day. In another embodiment, theamount laquinimod administered is 0.25 mg/day, 0.3 mg/day, 0.5 mg/day,0.6 mg/day, 1.0 mg/day, 1.2 mg/day, 1.5 mg/day or 2.0 mg/day. In yetanother embodiment, the amount of laquinimod administered is 0.05-4.0 mgper administration, 0.05-2.0 mg per administration, 0.2-4.0 mg peradministration, 0.2-2.0 mg per administration, about 0.1 mg peradministration, or about 0.5 mg per administration.

In one embodiment of the present invention, the method further comprisesadministration of a second agent for the treatment of glaucoma. Inanother embodiment, the second agent is a β-adrenergic antagonist,adrenergic agonist, parasympathomimetic, prostaglandin-like analog, orcarbonic anhydrase inhibitor.

In one embodiment, the periodic administration of laquinimod continuesfor at least 3 days, more than 30 days, more than 42 days, 8 weeks ormore, at least 12 weeks, at least 24 weeks, more than 24 weeks, or 6months or more. In another embodiment, the subject is a human patient.

The subject invention also provides a method of treating a subjectsuffering from retinal ganglion cell loss or retinal ganglion celldamage, or of reducing retinal ganglion cell loss or damage in asubject, comprising administering to the subject an amount of laquinimodeffective to reduce retinal ganglion cell loss or retinal ganglion celldamage in the subject.

The subject invention also provides a method of treating a subjectsuffering from elevated intraocular pressure, or of reducing intraocularpressure in a subject, comprising administering to the subject an amountof laquinimod effective to reduce intraocular pressure in the subject.

The subject invention also provides a package comprising a) apharmaceutical composition comprising an amount of laquinimod; and b)instruction for use of the pharmaceutical composition to treat a subjectafflicted with glaucoma.

In one embodiment of the present invention, the package comprises asecond pharmaceutical composition comprising an amount of a second agentfor the treatment of glaucoma. In another embodiment, the second agentis a β-adrenergic antagonist, adrenergic agonist, parasympathomimetic,prostaglandin-like analog, or carbonic anhydrase inhibitor.

In one embodiment, the pharmaceutical composition is the form of anaerosol, an inhalable powder, an injectable, a liquid, a gel, a solid, acapsule or a tablet. In another embodiment, the pharmaceuticalcomposition is in a liquid or a gel form.

In one embodiment, the concentration of laquinimod in the liquid or gelis 5-100 mg/ml solution, 20-100 mg/ml solution, 10-15 mg/ml solution or20-50 mg/ml solution.

In another embodiment, the pharmaceutical composition is in capsule formor in tablet form. In another embodiment, the tablets are coated with acoating which inhibits oxygen from contacting the core. In anotherembodiment, the coating comprises a cellulosic polymer, a detackifier, agloss enhancer, or pigment.

In one embodiment, the pharmaceutical composition further comprisesmannitol. In another embodiment, the pharmaceutical composition furthercomprises an alkalinizing agent. In another embodiment, the alkalinizingagent is meglumine. In another embodiment, the pharmaceuticalcomposition further comprises an oxidation reducing agent.

In one embodiment, the pharmaceutical composition is stable and free ofan alkalinizing agent or an oxidation reducing agent. In anotherembodiment, the pharmaceutical composition is free of an alkalinizingagent and free of an oxidation reducing agent.

In one embodiment, the pharmaceutical composition is stable and free ofdisintegrant. In another embodiment, the pharmaceutical compositionfurther comprises a lubricant. In another embodiment, the lubricant ispresent in the pharmaceutical composition as solid particles. In anotherembodiment, the lubricant is sodium stearyl fumarate or magnesiumstearate.

In one embodiment, the pharmaceutical composition further comprises afiller. In another embodiment, the filler is present in thepharmaceutical composition as solid particles. In another embodiment,the filler is lactose, lactose monohydrate, starch, isomalt, mannitol,sodium starch glycolate, sorbitol, lactose spray dried, lactoseanhydrouse, or a combination thereof. In another embodiment, the filleris mannitol or lactose monohydrate.

In one embodiment, the package further comprises a desiccant. In anotherembodiment, the desiccant is silica gel.

In one embodiment, the pharmaceutical composition is stable and has amoisture content of no more than 4%. In another embodiment, laquinimodis present in the pharmaceutical composition as solid particles. Inanother embodiment, the package is a sealed packaging having a moisturepermeability of not more than 15 mg/day per liter. In anotherembodiment, the sealed package is a blister pack in which the maximummoisture permeability is no more than 0.005 mg/day. In anotherembodiment, the sealed package is a bottle. In another embodiment, thebottle is closed with a heat induction liner. In another embodiment, thesealed package comprises an HDPE bottle. In another embodiment, thesealed package comprises an oxygen absorbing agent. In anotherembodiment, the oxygen absorbing agent is iron.

In one embodiment, the amount of laquinimod in the pharmaceuticalcomposition is at least 0.2 mg or less than 0.6 mg. In anotherembodiment, the amount of laquinimod in the pharmaceutical compositionis 0.1-40.0 mg, 0.03-600 mg, 0.1-2.5 mg, 0.25-2.0 mg, 0.5-1.2 mg, 0.25mg, 0.3 mg, 0.5 mg, 0.6 mg, 1.0 mg, 1.2 mg, 1.5 mg, or 2.0 mg. Inanother embodiment, the pharmaceutical composition comprises unit dosesof laquinimod of 0.05-4.0 mg, 0.05-2.0 mg, 0.2-4.0 mg, 0.2-2.0 mg, about0.1 mg, or about 0.5 mg.

In one embodiment, the pharmaceutical composition is formulated forintraocular, periocular, systemic or topical administration. In anotherembodiment, the pharmaceutical composition is formulated for oral orocular administration.

The subject invention also provides packages as described herein for usein treating a subject afflicted with glaucoma.

The subject invention also provides a therapeutic package for dispensingto, or for use in dispensing to, a subject afflicted with glaucoma,which comprises a) one or more unit doses, each such unit dosecomprising an amount of laquinimod thereof, wherein the amount of saidlaquinimod in said unit dose is effective, upon administration to saidsubject, to treat the subject, and b) a finished pharmaceuticalcontainer therefor, said container containing said unit dose or unitdoses, said container further containing or comprising labelingdirecting the use of said package in the treatment of said subject.

In one embodiment, the therapeutic package comprises a secondpharmaceutical composition comprising an amount of a second agent forthe treatment of glaucoma. In another embodiment, the second agent is aβ-adrenergic antagonist, adrenergic agonist, parasympathomimetic,prostaglandin-like analog, or carbonic anhydrase inhibitor.

The subject invention also provides a pharmaceutical compositioncomprising an amount of laquinimod for use in treating a subjectafflicted glaucoma.

In one embodiment, the pharmaceutical composition comprises an amount ofa second agent for the treatment of glaucoma. In another embodiment, thesecond agent is a β-adrenergic antagonist, adrenergic agonist,parasympathomimetic, prostaglandin-like analog, or carbonic anhydraseinhibitor.

In an embodiment, the pharmaceutical composition is in the form of anaerosol, an inhalable powder, an injectable, a liquid, a gel, a solid, acapsule or a tablet. In another embodiment, the pharmaceuticalcomposition is in a liquid or a gel form.

In an embodiment, the concentration of laquinimod in the liquid or gelis 5-100 mg/ml solution, 20-100 mg/ml solution, 10-15 mg/ml solution or20-50 mg/ml solution. In another embodiment, the pharmaceuticalcomposition comprises a unit dose of 10 μL of an aqueous pharmaceuticalsolution which contains in solution at least 0.2 mg laquinimod. Inanother embodiment, laquinimod is laquinimod sodium.

In one embodiment, the pharmaceutical composition is in capsule form orin tablet form. In another embodiment, the tablets are coated with acoating which inhibits oxygen from contacting the core. In anotherembodiment, the coating comprises a cellulosic polymer, a detackifier, agloss enhancer, or pigment. In another embodiment, the pharmaceuticalcomposition further comprises mannitol.

In one embodiment, the pharmaceutical composition further comprises analkalinizing agent. In another embodiment, the alkalinizing agent ismeglumine. In another embodiment, the pharmaceutical composition furthercomprises an oxidation reducing agent.

In one embodiment, the pharmaceutical composition is free of analkalinizing agent or an oxidation reducing agent. In anotherembodiment, the pharmaceutical composition is free of an alkalinizingagent and free of an oxidation reducing agent.

In one embodiment, the pharmaceutical composition is stable and free ofdisintegrant. In another embodiment, the pharmaceutical compositionfurther comprises a lubricant. In another embodiment, the lubricant ispresent in the pharmaceutical composition as solid particles. In anotherembodiment, the lubricant is sodium stearyl fumarate or magnesiumstearate.

In one embodiment, the pharmaceutical composition further comprises afiller. In another embodiment, the filler is present in thepharmaceutical composition as solid particles. In another embodiment,the filler is lactose, lactose monohydrate, starch, isomalt, mannitol,sodium starch glycolate, sorbitol, lactose spray dried, lactoseanhydrouse, or a combination thereof. In another embodiment, the filleris mannitol or lactose monohydrate.

In one embodiment, the amount of laquinimod in the pharmaceuticalcomposition is at least 0.2 mg or less than 0.6 mg. In anotherembodiment, the amount of laquinimod in is 0.1-40.0 mg, 0.03-600 mg,0.1-2.5 mg, 0.25-2.0 mg, 0.5-1.2 mg, 0.25 mg, 0.3 mg, 0.5 mg, 0.6 mg,1.0 mg, 1.2 mg, 1.5 mg, or 2.0 mg. In another embodiment, thepharmaceutical composition comprises unit doses of laquinimod of0.05-4.0 mg, 0.05-2.0 mg, 0.2-4.0 mg, 0.2-2.0 mg, about 0.1 mg, or about0.5 mg.

In one embodiment, the pharmaceutical composition is formulated forintraocular, periocular, systemic or topical administration. In anotherembodiment, the pharmaceutical composition is formulated for oral orocular administration.

The subject invention also provides a pharmaceutical composition asdescribed herein for use in treating a subject afflicted with glaucoma.

The subject invention also provides a pharmaceutical composition in unitdosage form, useful in treating a subject afflicted with glaucoma, whichcomprises an amount of laquinimod; which amount of said laquinimod insaid composition is effective, upon administration to said subject ofone or more of said unit dosage forms of said composition, to treat thesubject.

The subject invention also provides a package comprising a) apharmaceutical composition as described herein; and b) instruction foruse of the pharmaceutical composition to treat a subject afflicted withglaucoma.

The subject invention also provides laquinimod for the manufacture of amedicament for use in treating a subject afflicted glaucoma.

For the foregoing embodiments, each embodiment disclosed herein iscontemplated as being applicable to each of the other disclosedembodiments. For instance, the elements recited in the methodembodiments can be used in the pharmaceutical composition, package, anduse embodiments described herein and vice versa.

Terms

As used herein, and unless stated otherwise, each of the following termsshall have the definition set forth below.

As used herein, “laquinimod” means laquinimod acid or a pharmaceuticallyacceptable salt thereof.

A “salt thereof” is a salt of the instant compounds which have beenmodified by making acid or base salts of the compounds. The term“pharmaceutically acceptable salt” in this respect, refers to therelatively non-toxic, inorganic and organic acid or base addition saltsof compounds of the present invention. For example, one means ofpreparing such a salt is by treating a compound of the present inventionwith an inorganic base.

As used herein, an “amount” or “dose” of laquinimod as measured inmilligrams refers to the milligrams of laquinimod acid present in apreparation, regardless of the form of the preparation. A “dose of 0.6mg laquinimod” means the amount of laquinimod acid in a preparation is0.6 mg, regardless of the form of the preparation. Thus, when in theform of a salt, e.g. a laquinimod sodium salt, the weight of the saltform necessary to provide a dose of 0.6 mg laquinimod would be greaterthan 0.6 mg (e.g., 0.64 mg) due to the presence of the additional saltion.

As used herein, a “unit dose”, “unit doses” and “unit dosage form(s)”mean a single drug administration entity/entities.

As used herein, “about” in the context of a numerical value or rangemeans ±10% of the numerical value or range recited or claimed.

As used herein, a composition that is “free” of a chemical entity meansthat the composition contains, if at all, an amount of the chemicalentity which cannot be avoided although the chemical entity is not partof the formulation and was not affirmatively added during any part ofthe manufacturing process. For example, a composition which is “free” ofan alkalizing agent means that the alkalizing agent, if present at all,is a minority component of the composition by weight. Preferably, when acomposition is “free” of a component, the composition comprises lessthan 0.1 wt %, 0.05 wt %, 0.02 wt %, or 0.01 wt % of the component.

As used herein, “alkalizing agent” is used interchangeably with the term“alkaline-reacting component” or “alkaline agent” and refers to anypharmaceutically acceptable excipient which neutralizes protons in, andraises the pH of, the pharmaceutical composition in which it is used.

As used herein, “oxidation reducing agent” refers to a group ofchemicals which includes an “antioxidant”, a “reduction agent” and a“chelating agent”.

As used herein, “antioxidant” refers to a compound selected from thegroup consisting of tocopherol, methionine, glutathione, tocotrienol,dimethyl glycine, betaine, butylated hydroxyanisole, butylatedhydroxytoluene, turmerin, vitamin E, ascorbyl palmitate, tocopherol,deteroxime mesylate, methyl paraben, ethyl paraben, butylatedhydroxyanisole, butylated hydroxytoluene, propyl gallate, sodium orpotassium metabisulfite, sodium or potassium sulfite, alpha tocopherolor derivatives thereof, sodium ascorbate, disodium edentate, BHA(butylated hydroxyanisole), a pharmaceutically acceptable salt or esterof the mentioned compounds, and mixtures thereof.

The term “antioxidant” as used herein also refers to Flavonoids such asthose selected from the group of quercetin, morin, naringenin andhesperetin, taxifolin, afzelin, quercitrin, myricitrin, genistein,apigenin and biochanin A, flavone, flavopiridol, isoflavonoids such asthe soy isoflavonoid, genistein, catechins such as the tea catechinepigallocatechin gallate, flavonol, epicatechin, hesperetin, chrysin,diosmin, hesperidin, luteolin, and rutin.

As used herein, “reduction agent” refers to a compound selected from thegroup consisting of thiol-containing compound, thioglycerol,mercaptoethanol, thioglycol, thiodiglycol, cysteine, thioglucose,dithiothreitol (DTT), dithio-bis-maleimidoethane (DTME),2,6-di-tert-butyl-4-methylphenol (BHT), sodium dithionite, sodiumbisulphite, formamidine sodium metabisulphite, and ammonium bisulphite.”

As used herein, “chelating agent” refers to a compound selected from thegroup consisting of penicillamine, trientine,N,N′-diethyldithiocarbamate (DDC), 2,3,2′-tetraamine (2,3,2′-tet),neocuproine, N,N,N′,N′-tetrakis(2-pyridylmethyl)ethylenediamine (TPEN),1,10-phenanthroline (PHE), tetraethylenepentamine, triethylenetetraamineand tris(2-carboxyethyl) phosphine (TCEP), ferrioxamine, CP94, EDTA,deferoxainine B (DFO) as the methanesulfonate salt (also known asdesferrioxanilne B mesylate (DFOM)), des feral from Novartis (previouslyCiba-Giegy), and apoferritin.

As used herein, a pharmaceutical composition is “stable” when thecomposition preserves the physical stability/integrity and/or chemicalstability/integrity of the active pharmaceutical ingredient duringstorage. Furthermore, “stable pharmaceutical composition” ischaracterized by its level of degradation products not exceeding 5% at40° C./75%RH after 6 months or 3% at 55° C./75% RH after two weeks,compared to their level in time zero.

As used herein, “effective” when referring to an amount of laquinimodrefers to the quantity of laquinimod that is sufficient to yield adesired therapeutic response. Efficacy can be measured by e.g., areduced intraocular pressure (IOP).

Administering to the subject” or “administering to the (human) patient”means the giving of, dispensing of, or application of medicines, drugs,or remedies to a subject/patient to relieve, cure, or reduce thesymptoms associated with a condition, e.g., a pathological condition.The administration can be periodic administration. As used herein,“periodic administration” means repeated/recurrent administrationseparated by a period of time. The period of time betweenadministrations is preferably consistent from time to time. Periodicadministration can include administration, e.g., once daily, twicedaily, three times daily, four times daily, weekly, twice weekly, threetimes weekly, four times weekly and so on, etc.

The route of administration can be, e.g., topical. Routes ofadministration can also be classified by whether the effect is local(e.g., in topical administration) or systemic (e.g., in enteral orparenteral administration). “Local administration” as used herein shallmean administration of a compound or composition directly to where itsaction is desired, and specifically excludes systemic administration.“Topical administration” of a compound or composition as used hereinshall mean application of the compound or composition to body surfacessuch as the skin or mucous membranes such as eyes. “Ocularadministration” as used herein shall mean application of a compound orcomposition to the eye of a subject or to the skin around the eye(periocular skin) of a subject, i.e., local administration. Examples ofocular administration include topical administration directly to theeye, topical application to the eye lid or injection into a portion ofthe eye or eye socket. In addition, an “ocular pharmaceuticalcomposition” as used herein means a pharmaceutical compositionformulated for ocular administration.

“Treating” as used herein encompasses, e.g., inducing inhibition,regression, or stasis of a disease or disorder, e.g., glaucoma, oralleviating, lessening, suppressing, inhibiting, reducing the severityof, eliminating or substantially eliminating, or ameliorating a symptomof the disease or disorder.

“Inhibition” of disease progression or disease complication in a subjectmeans preventing or reducing the disease progression and/or diseasecomplication in the subject.

A “symptom” associated with glaucoma includes any clinical or laboratorymanifestation associated with glaucoma and is not limited to what thesubject can feel or observe.

As used herein, a subject “afflicted” with glaucoma means the subjecthas been diagnosed with glaucoma.

As used herein, a subject at “baseline” is as subject prior toadministration of laquinimod in a therapy as described herein.

A “pharmaceutically acceptable carrier” refers to a carrier or excipientthat is suitable for use with humans and/or animals without undueadverse side effects (such as toxicity, irritation, and allergicresponse) commensurate with a reasonable benefit/risk ratio. It can be apharmaceutically acceptable solvent, suspending agent or vehicle, fordelivering the instant compounds to the subject.

It is understood that where a parameter range is provided, all integerswithin that range, and tenths thereof, are also provided by theinvention. For example, “0.1-2.5 mg/day” includes 0.1 mg/day, 0.2mg/day, 0.3 mg/day, etc. up to 2.5 mg/day.

This invention will be better understood by reference to theExperimental Details which follow, but those skilled in the art willreadily appreciate that the specific experiments detailed are onlyillustrative of the invention as described more fully in the claimswhich follow thereafter.

Experimental Details EXAMPLE 1 Assessment Of The NeuroprotectiveEfficacy of Laquinimod For The Retinal Ganglion Cell (RGC) Survival In ARat Glaucoma Model

The purpose of this study was to assess the efficacy of laquinimod inprotecting against chronic ocular hypertension (OHT) and RGCdegeneration in a rat model of glaucoma, created by injecting hypertonicsaline into the episcleral veins in one eye of the Brown Norway rat. Inthis model, RGC degeneration occurs in response to increased IOP and OHTsimilar to that in human patients with glaucoma.

SUMMARY

The study included 5 groups (n=8 each): Group 1 (1% Laquinimod fortopical administration), Group 2 (Vehicle for topical administration),Group 3 (4% Laquinimod for topical administration), Group 4 (0.25%Laquinimod for topical administration) and Group 5 (0.1% Laquinimod fororal administration).

Prior to any experimental procedure, clinical observations wereperformed daily, body weights were obtained, intraocular pressure (IOP)was measured and detailed ocular examinations were performed on botheyes. Animals that were found to be clinically normal with no baselineocular abnormalities were selected for use in the study.

The rat model of chronic ocular hypertension (OHT)/glaucoma was createdin the left eye of each animal via two hypertonic saline injections(HSI) each one week apart. The un-injected right eye served as thecontrol. Throughout the study, the vehicle control and the test articleswere prepared weekly.

Rats were dosed once daily for oral administration (Group 5) and twicedaily for topical administration groups (Groups 1-4), starting on theday of the first HSI until euthanasia. Detailed ocular examinations wereperformed one week after the 2nd HSI and on the day of euthanasia.Approximately one week prior to euthanasia, RGCs wereretrogradely-labeled by bilateral injections of Fluoro-Gold (FG) intothe superior colliculus in the brain. Post-dose IOP was measured weeklyfor 5 weeks starting one week after the 2nd HSI until euthanasia.

For each IOP measurement time-point following the 2nd HSI, the IOPelevation was calculated as the difference between the IOP in the lefteye with OHT and that in the non-OHT right eye (ΔIOP). The ΔIOP for the5 weekly post-HSI IOP measurements were averaged and constituted theMean ΔIOP for each animal. Rats which did not have individual IOPmeasurements of ≧50 mmHg in the OHT eyes were selected from a largerpool and groups (n=8 each) were matched for the Mean ΔIOP. Other animalswere removed from the study.

Animals were euthanized 5 weeks after the 2nd HSI. The retinas wereflat-mounted, slide IDs were masked and 8 regions per retina were imagedusing a confocal microscope. RGC at these regions were counted using theImage J software. After the optic nerves were extracted, they wereplastic-embedded, sectioned and stained with Toluidine Blue at SchepensEye Research Institute, Boston, Mass. The injury in the optic nerves wasevaluated and graded by microscopic examination in a masked fashion.

There were no abnormal clinical signs or ocular abnormalities noted inany of the 40 animals in the beginning of the study.

There were no treatment-related findings in the clinical observations orocular examinations during the study in any of the animals.

A One-Way ANOVA indicated that the group body weights were notstatistically different on the day of dosing among groups (P =0.957).Groups also did not differ in the amount of weight gained between theday of dosing and the day of euthanasia (One-Way ANOVA; P=0.559). Forfive weeks post-dose, the mean ΔIOP values (OHT—Non-OHT) (Mean±SD) were9.1±2.2 mmHg, 9.1±2.6 mmHg, 9.3±2.7 mmHg, 9.2±1.5 mmHg, and 9.1±2.9 mmHgfor Groups 1, 2, 3, 4 and 5, respectively. A One-Way ANOVA analysisindicated that the groups were well-matched for Mean ΔIOP (P>0.9).Compared to the non-OHT retinas, % Fluoro-gold labeled—RGC Loss(Mean±SD) in the OHT retinas was 17.6±33.8, 34.8±42.7, 26.8±36.4,21.6±21.7, and 22.9±33.1 for Groups 1, 2, 3, 4 and 5, respectively.FG—Labeled RGC counts per mm² were compared between the Non-OHT and theOHT retinas for each group using two-tailed paired-t tests. Group 2(vehicle topical; P=0.047) and Group 4 (0.25% Laquinimod topical;P=0.033) had fewer RGCs in the OHT eye compared to the Non-OHT eyes. Thenumber of RGCs in Group 3 (4% Laquinimod topical; P=0.071) and Group 5(0.1% Laquinimod oral; P=0.075) were statistically different between theOHT and Non-OHT eyes. However, in Group 1 (1% Laquinimod topical), therewas no statistically significant difference in the RGC counts betweenthe OHT and Non-OHT eyes (P=0.189). This suggests that the daily topicalapplication of 1% Laquinimod may be neuroprotective for the RGC. For theoptic nerves in the Non-OHT (control) eyes, the Mean Injury Grades(Mean±SD) were 1.1±0.1, 1.2±0.2, 1.2±0.2, 1.2±0.3 and 1.2±0.2 for Groups1, 2, 3, 4 and 5, respectively. For the optic nerves in the OHT eyes,the Mean Injury Grades (Mean±SD) for the OHT optic nerves were 2.5±1.3,3.0±1.6, 3.0±1.5, 2.8±1.3 and 2.7±1.5 for Groups 1, 2, 3, 4, and 5respectively. As a secondary analysis, Mean ON Injury Grades werecompared between the Non-OHT and the OHT optic nerves for each groupusing two-tailed paired-t tests. The Mean ON injury grades weresignificantly greater in the OHT eyes compared to the Non-OHT controleyes in all groups (P<0.05).

Materials

Test Article: laquinimod sodium stored at room temperature protectedfrom light.

Control Article: 0% laquinimod sodium stored under refrigeration.

Animals

Number and Species: The study quote and outline-specified data werecollected on 40 Brown Norway rats (Rattus norvegicus). Rats have beenused historically as OHT models and there are no other approvedalternative (non-animal methods). The study started with 90 animals toensure that sufficient data were available at the end of the study.

Sex: Male

Weight/Age Range: approximately 271.2-366.4 grams/at least 12 weeks old(adult) weighed to nearest 0.1 g.

Procedure

Ocular and oral exposure corresponds to the route of human exposure. Forthe four topical administration groups, the test and control articleswere applied topically to the surface of one eye of the test system. Thetest article was administered orally for the fifth group of animals.

Preparation of Test and Control Articles

All test and control articles were prepared as described below. Thefinal volume for the formulations described below is 200 mL but theformulations were proportionally changed to the required volume for eachpreparation. Three different concentrations (0.25%, 1%, and 4%) of thetest article for topical application and the test article for oralgavage (0.1%) were prepared weekly. The control article for topicalapplication was also prepared weekly. The identification of the test andcontrol articles for the topical administration was masked afterpreparation of the topical formulations.

TABLE 1 LAQ 4.0% Topical Formulation (40 mg/mL of LAQ) Material g/200 mLsolution Laquinimod Sodium 8.52 (equivalent to 8 g Laquinimod acid)Sodium Phosphate Dibasic 7 Hydrate 2.497 Sodium Phosphate MonobasicMonohydrate 0.0942 Hydroxy Ethyl Cellulose (HEC) HX 0.3 Water forInjection Amount required to bring solution to 200 mL

Table 1 Process:

-   -   1. The entire process is performed under yellow light or at dark        conditions.    -   2. Weigh 175 g (175 mL) of water for injection in a glass        container containing a stirrer.    -   3. Weigh and add the Sodium Phosphate Monobasic Monohydrate and        Sodium Phosphate Dibasic 7 Hydrate and stir for approximately 5        minutes. Verify complete dissolution by visual inspection of a        clear transparent solution.    -   4. Measure the pH (Approximately 7.7-8.3).    -   5. Weigh and add Laquinimod Sodium to the solution. Rinse the        weighing boat from the Laquinimod Sodium remaining with ˜5 mL of        water and to the solution. Stir for approximately 5 minutes and        verify complete dissolution by visual inspection of a clear        transparent solution.    -   6. Weigh and add the Hydroxy Ethyl Cellulose HX.    -   7. Stir for approximately 2 hours.    -   8. Remove the stirrer and add the solution to a 200 mL        volumetric flask.    -   9. Add water for injection up to 200 mL.    -   10. Shake manually for approximately two minutes.    -   11. Transfer into an appropriate container. Wrap with aluminum        foil and keep the solution refrigerated.

TABLE 2 LAQ 1.0% Topical Formulation (10 mg/mL of LAQ) Material g/200 mLsolution Laquinimod Sodium 2.12 (equivalent to 2 g Laquinimod acid)Sodium Phosphate Dibasic 7 Hydrate 2.497 Sodium Phosphate MonobasicMonohydrate 0.0942 Hydroxy Ethyl Cellulose (HEC) HX 0.3 Sodium chloride0.75 Water for Injection Amount required to bring solution to 200 mL

Table 2 Process:

-   -   1. The entire process is performed under yellow light or at dark        conditions.    -   2. Weigh 175 g (175 mL) of water for injection in a glass        container containing a stirrer.    -   3. Weigh and add the Sodium Phosphate Monobasic Monohydrate and        Sodium Phosphate Dibasic 7 Hydrate and stir for approximately 5        minutes. Verify complete dissolution by visual inspection of a        clear transparent solution.    -   4. Measure the pH (Approximately 7.7 to 8.3).    -   5. Weigh and add Laquinimod Sodium to the solution. Rinse the        weighing boat from the Laquinimod Sodium remaining with ˜5 mL of        water and to the solution. Stir for approximately 5 minutes and        verify complete dissolution by visual inspection of a clear        transparent solution.    -   6. Weigh and add the Sodium Chloride to the solution. Stir for        approximately 2 minutes. Verify complete dissolution by visual        inspection of a clear transparent solution.    -   7. Weigh and add the Hydroxy Ethyl Cellulose HX.    -   8. Stir for approximately 2 hours.    -   9. Remove the stirrer and add the solution to a 200 mL        volumetric flask.    -   10. Add water for injection up to 200 mL.    -   11. Shake manually for approximately two minutes.    -   12. Transfer into an appropriate container. Wrap with aluminum        foil and keep the solution refrigerated.

TABLE 3 LAQ 0.25% Topical Formulation (2.5 mg/mL of LAQ) Material g/200mL solution Laquinimod Sodium 0.54 (equivalent to 0.5 g Laquinimod acid)Sodium Phosphate Dibasic 7 Hydrate 2.497 Sodium Phosphate MonobasicMonohydrate 0.0942 Hydroxy Ethyl Cellulose (HEC) HX 0.3 Sodium chloride0.94 Water for Injection Amount required to bring solution to 200 mL

Table 3 Process:

-   -   1. The entire process is performed under yellow light or at dark        conditions.    -   2. Weigh 175 g (175 mL) of water for injection in a glass        container containing a stirrer.    -   3. Weigh and add the Sodium Phosphate Monobasic Monohydrate and        Sodium Phosphate Dibasic 7 Hydrate and stir for approximately 5        minutes. Verify complete dissolution by visual inspection of a        clear transparent solution.    -   4. Measure the pH (Approximately 7.7-8.3).    -   5. Weigh and add Laquinimod Sodium to the solution. Rinse the        weighing boat from the Laquinimod Sodium remaining with ˜5 mL of        water and to the solution. Stir for approximately 5 minutes and        verify complete dissolution by visual inspection of a clear        transparent solution.    -   6. Weigh and add the Sodium Chloride to the solution. Stir for        approximately 2 minutes. Verify complete dissolution by visual        inspection of a clear transparent solution.    -   7. Weigh and add the Hydroxy Ethyl Cellulose HX.    -   8. Stir for approximately 2 hours.    -   9. Remove the stirrer and add the solution to a 200 mL        volumetric flask.    -   10. Add water for injection up to 200 mL.    -   11. Shake manually for approximately two minutes.    -   12. Transfer into an appropriate container. Wrap with aluminum        foil and keep the solution refrigerated.

TABLE 4 LAQ 0% Topical Formulation (Control Article) Material g/200 mLsolution Sodium Phosphate Dibasic 7 Hydrate 2.497 Sodium PhosphateMonobasic Monohydrate 0.0942 Hydroxy Ethyl Cellulose (HEC) HX 0.3 Sodiumchloride 1 Water for Injection Amount required to bring solution to 200mL

Table 4 Process:

-   -   1. The entire process is performed under yellow light or at dark        conditions.    -   2. Weigh 175 g (175 mL) of water for injection in a glass        container containing a stirrer.    -   3. Weigh and add the Sodium Phosphate Monobasic Monohydrate and        Sodium Phosphate Dibasic 7 Hydrate and stir for approximately 5        minutes. Verify complete dissolution by visual inspection of a        clear transparent solution.    -   4. Measure the pH (Approximately 7.7 to 8.3).    -   5. Weigh and add the Sodium Chloride to the solution. Stir for        approximately 2 minutes. Verify complete dissolution by visual        inspection of a clear transparent solution.    -   6. Weigh and add the Hydroxy Ethyl Cellulose HX.    -   7. Stir for approximately 2 hours.    -   8. Remove the stirrer and add the solution to a 200 mL        volumetric flask.    -   9. Add water for injection up to 200 mL.    -   10. Shake manually for approximately two minutes.    -   11. Transfer into an appropriate container.

TABLE 5 LAQ 0.1% Oral Formulation (1.0 mg/mL of LAQ) Material g/200 mLsolution Laquinimod Sodium 0.2 (Equivalent to 0.2 g laquinimod acid)Autoclaved Tap Water Amount required to bring solution to 200 mL

Table 5 Process:

-   -   1. The entire process is performed under yellow light or at dark        conditions.    -   2. Weigh 150 g (150 mL) of autoclaved tap water in a glass        container containing a stirrer.    -   3. Weigh and add Laquinimod Sodium to the solution. Rinse the        remaining Laquinimod Sodium in the weighing boat with ˜5 mL of        water and add to the solution. Stir for approximately 5 minutes        and verify complete dissolution by visual inspection of a clear        transparent solution.    -   4. Add autoclaved tap water up to 200 mL.    -   5. Stir for 5 minutes.    -   6. Transfer into an appropriate amber Pre-Dose Administration        and Selection of Animals:

Clinical observations were performed daily according to Table 6 below:

TABLE 6 Clinical Signs and Observations Observed Sign Involved System(s)Respiratory Dyspnea (abdominal breathing, CNS, pulmonary, cardiacgasping), apnea, cyanosis, tachypnea, nostril discharges MotorActivities Decrease/increase somnolence, CNS, somatomotor, sensory, lossof righting, anaesthesia, neuromuscular, autonomic catalepsy, ataxia,unusual locomotion, prostration, tremors, fasciculation ConvulsionClonic, tonic, tonic-clonic, CNS, neuromuscular, autonomic, asphyxial,opisthotonos respiratory Reflexes Corneal, righting, myotact, light,CNS, sensory, autonomic, startle reflex neuromuscular Ocular SignsLacrimation, miosis, mydriasis, Autonomic, irritation exophthalmos,ptosis, opacity, iritis, conjunctivitis, chromodacryorrhea, relaxationof nictitating membrane Cardiovascular Signs Bradycardia, tachycardia,CNS, autonomic, cardiac, arrhythmia, vasodilation, pulmonaryvasoconstriction Salivation Excessive Autonomic Piloerection Rough hairAutonomic Analgesia Decrease reaction CNS, sensory Muscle ToneHypotonia, hypertonia Autonomic Gastrointestinal Soft stool, diarrhea,emesis, CNS, autonomic, sensory, GI diuresis, erythruria motility,kidney Skin Edema, erythema Tissue damage, irritation

Animals were weighed weekly prior to initiation of dosing. The first daythe rats are weighed was designated as Study Day 1, and the beginning ofStudy Week 1.

Ophthalmic Examinations:

Animals selected for the study were examined prior to the initialadministration of the test or the control articles to ensure that botheyes were free of abnormality, damage, and disease. Both eyes wereexamined, scored and recorded prior to the initial dose administrationusing a hand held slit-lamp and a direct ophthalmoscope or the surgicalmicroscope according to the Classification System for Grading OcularLesions as described in Table 7, and the Ocular Posterior SegmentScoring Scale of Table 8. Posterior segment examination was performedafter topical application of Tropicamide in the conscious state, orafter the rats are anesthetized with isoflorane inhalation. Only ratsshowing no signs of eye irritation, ocular defects, or preexistingcorneal injury were used in the study.

TABLE 7 Combined Draize and McDonald-Shadduck Scoring System CONJUNCTIVAA. REDNESS/CONGESTION 0 Vessels normal. May appear blanched to reddishpink without perilimbal injection (except at 12:00 and 6:00 o'clockpositions) with vessels of the palpebral and bulbar conjunctivae easilyobserved. 1 Vessels definitely injected above normal. A flushed, reddishcolor predominately confined to the palpebral conjunctivae with someperilimbal injection but primarily confined to the lower and upper partsof the eye from, the 4:00 and 7:00 and 11:00 to 1:00 o'clock positions.2*† More diffuse, deeper crimson red, individual vessels not easilydiscernible. Bright red color of the palpebral conjunctiva withaccompanying perilimbar injection covering at least 75% of thecircumference of the perilimbal region. 3*† Diffuse beefy red. Darkbeefy red color with congestion of both the bulbar and palpebralconjunctiva along with pronounced perilimbal injection and the presenceof petechia on the conjunctiva. The B. CHEMOSIS: 0 Normal. No swellingof the conjunctival tissue. 1 Any swelling above normal (includesnictitating membrane). Swelling above normal without eversion of thelids (can be easily ascertained by noting that the upper and lowereyelids are positioned as in the normal eye); swelling generally startsin the lower cul-de-sac near the inner canthus which needs slit-lampexamination. 2*† Obvious swelling with partial eversion of lids.Swelling with misalignment of the normal approximation of the lower andupper eyelids; primarily confined to the upper eyelid so that in theinitial stages the misapproximation of the eyelids begins by partialeversion of the upper eyelid. In this stage, swelling is confinedgenerally to the upper eyelid, although it exists in the lowercul-de-sac. Swelling with lids about half closed. 3*† Swelling definitewith partial eversion of the upper and lower eyelids essentiallyequivalent. This can be easily ascertained by looking at the animalstraight head on and noticing the positioning of the eyelids; if the eyemargins do not meet, eversion has occurred. 4*† Swelling with lids abouthalf closed to completely closed. Eversion of the upper eyelid ispronounced with less pronounced eversion of the lower eyelid. It isdifficult to retract the lids and observe the perilimbal region. C.DISCHARGE: 0 Normal or no discharge. 1 Any amount different from normal(does not include small amounts observed in inner canthus of normalanimals). Discharge above normal and present on the inner portion of theeye but not on the lids or hairs of the eyelids. One can ignore thesmall amount that is in the inner and outer canthus if it has not beenremoved prior to starting the study. 2 Discharge with moistening of lidsand hairs just adjacent to lids. Discharge is abundant, easily observed,and has collected on the lids around the hairs of the eyelids. 3Discharge with moistening of the lids and hairs, and considerable areaaround the eye. CORNEA D. OPACITY-degree of density (areas most densetaken for reading): 0 No ulceration or opacity. Normal cornea. Appearswith the slit lamp as having a bright gray line on the endothelialsurface and a bright gray line on the endothelial surface with amarble-like gray appearance of the stroma. 1* Scattered or diffuse areasof opacity (other than slight dulling of normal luster), details of irisclearly visible. Some loss of transparency. Only the anterior one-halfof the stroma is involved as observed with an optical section of theslit lamp. The underlying structures are clearly visible with diffuseillumination, although some cloudiness can be readily apparent withdiffuse illumination. 2*† Easily discernible translucent areas, detailsof iris slightly obscured. Moderate loss of transparency. In addition toinvolving the anterior stroma, the cloudiness extends all the way to theendothelium. The stroma has lost its marble-like appearance and ishomogeneously white. With diffuse illumination, underlying structuresare clearly visible. 3*† Opalescent/nacreous areas, no details of irisvisible, size of pupil barely discernible. Involvement of the entirethickness of the stroma. With optical section, the endothelial surfaceis still visible. However, with diffuse illumination the underlyingstructures are just barely visible (to the extent that the observer isstill able to grade flare, iritis, observe for pupillary response, andnote lenticular changes. 4*† Opaque cornea, iris not discernible throughopacity. Involvement of the entire thickness of the stroma. With theoptical section, cannot clearly visualize the endothelium. With diffuseillumination, the underlying structures cannot be seen. Cloudinessremoves the capability of judging and grading aqueous flare, iritis,lenticular changes, and pupillary response. E. AREAS OF CORNEA INVOLVED:0 Normal cornea with no area of cloudiness. 1 One-quarter (or less), butnot zero. 2 Greater than one-quarter, but less than one-half. 3* Greaterthan one-half, but less than three-quarters. 4* Greater thanthree-quarters, up to whole area. F. FLUORESCEIN STAINING: 0 Absence offluorescein staining. 1 Slight fluorescein staining confined to a smallfocus. With diffuse illumination the underlying structures are easilyvisible. The outline of the papillary margin is as if there were nofluorescein staining. 2 Moderate fluorescein staining confined to asmall focus. With diffuse illumination the underlying structures areclearly visible, although there is some loss of detail. 3 Markedfluorescein staining. Staining may involve a larger portion of thecornea. With diffuse illumination the underlying structures are barelyvisible but are not completely obliterated. 4 Extreme fluoresceinstaining. With diffuse illumination the underlying structures cannot beobserved. G. CORNEA PANNUS: 0 No pannus 1 Vascularization is present butvessels have not invaded the entire corneal circumference. Wherelocalized vessel invasion has occurred, they have not penetrated beyond2 mm. 2 Vessels have invaded 2 mm or more around the entire cornealcircumference. IRIS 0 Normal iris without any hyperemia of the irisvessels. Occasionally around the 12:00 to 1:00 position near thepupillary border and the 6:00 and 7:00 position near the pupillaryborder there is a small area around 1-3 mm in diameter in which both thesecondary and tertiary vessels are slightly hyperemic. 1*† Folds abovenormal, congestion, swelling, circumcorneal injection (any or all ofthese or combination of any thereof), iris still reacting to light(sluggish reaction is positive). Minimal injection of secondary vesselsbut not tertiary. Generally, it is uniform, but may be of greaterintensity at the 1:00 or 6:00 position, the tertiary vessels must besubstantially hyperemic. 2*† No reaction to light, hemorrhage, grossdestruction (any or all of these). Minimal injection of tertiary vesselsand minimal to moderate injection of the secondary vessels. 3*† Moderateinjection of the secondary and tertiary vessels with slight swelling ofthe iris stroma (this gives the iris surface a slightly ruposeappearance which is usually most prominent near the 3:00 and 9:00positions). 4*† Marked injection of the secondary and tertiary vesselswith marked swelling of the iris stroma. The iris appears rugose; may beaccompanied by hemorrhage (hyperemia) in the anterior chamber. AQUEOUSFLARE 0 Absence of visible light beam in the anterior chamber (noTyndall effect). 1 Tyndall effect is barely discernible. The intensityof the light beam in the anterior chamber is less than the density ofthe slit beam as it passes through the lens. 2 The Tyndall effect in theanterior chamber is easily discernible and is of equal intensity as thedensity of the slit beam as it passes through the lens. 3 The Tyndalleffect in the anterior chamber is easily discernible; its intensity isgreater than the intensity of the slit beam as it passes through thelens. PUPILLARY LIGHT REFLEX: 0 Normal pupillary light reflex 1 Sluggishpupillary light reflex 2 No pupillary light reflex LENS 0 Normal 1 Thepresence of lenticular opacities should be described and the locationnoted as defined below:  Anterior capsule  Anterior subcapsule  Anteriorcortical  Nuclear  Posterior cortical  Posterior subcapsule  Posteriorcapsule *= Positive Reaction (ISO) †= Positive Reaction (OECD)

TABLE 8 Ocular Posterior Segment Scoring Scale VITREOUS BODY 0 Normal,the vitreous body is clear or transparent. 1 Abnormal, the vitreous bodyis not clear or not transparent and homogenous gel that fills the spacebetween the posterior axial lens capsule, posterior chamber, and ocularfundus. OPTIC DISC/OPTIC NERVE 0 Normal, the optic disc and optic nerveare with light red color, cupping size normal (cup-to-disc ratio <0.2),and normal sharpness of edge, without swelling, hemorrhages, notching inthe optic disc and any other unusual anomalies. 1 Abnormal, the opticdisc and optic nerve are not with light red color or cupping size normal(cup-to-disc ratio >0.2), and no normal sharpness of edge or withswelling, hemorrhages, notching in the optic disc and any other unusualanomalies. RETINAL BLOOD VASCULATURE 0 Normal, the retinal arteries andveins fill in blood and normalize sharpness without hemorrhage andexudation. 1 Abnormal, the retinal arteries and veins don't fill inblood and don't have normalize sharpness or with hemorrhage andexudation. RETINAL HEMORHAGE, EXUDATION, AND DETACHMENT 0 Normal retinawith no area of hemorrhage or/and exudation or/and detachment 1 Retinalhemorrhage or/and exudation or/and detachment ≦1 quadrant area 2 1quadrant area < retinal hemorrhage or/and exudation or/and detachment ≦2quadrant areas 3 2 quadrant areas < hemorrhage or/and exudation or/anddetachment ≦3 quadrant areas 4 3 quadrant areas < retinal hemorrhageor/and exudation or/and detachment exudation ≦4 quadrant areas CHOROIDALHEMORRHAGE, EXUDATION, AND DETACHMENT 0 Normal choroid with no area ofchoroidal and hemorrhage or/and exudation or/and detachment 1 Choroidalhemorrhage or/and exudation or/and detachment ≦1 quadrant area 2quadrant area < Choroidal hemorrhage or/and exudation or/and detachment≦2 quadrant areas 3 2 quadrant areas < Choroidal hemorrhage or/andexudation or/and detachment ≦3 quadrant areas 4 quadrant areas <Choroidal hemorrhage or/and exudation or/and detachment ≦4 quadrant area

Intraocular Pressure (IOP) Measurements:

Baseline IOP measurements were taken before the initial doseadministration. After application of topical anesthesia (0.5%Proparacaine HCl Ophthalmic Solution), IOP was measured on consciousrats on both eyes using a Tono-Pen Vet tonometer (Reichert, Inc.; Depew,N.Y.). Ten (10) IOP readings are recorded from each eye and averaged.IOP measurements were taken around the same time (e.g., between 10 a.m.and 2 p.m.) across measurement time-points to minimize the circadianvariability of IOP.

Dose Administration:

Rats were separated in 5 groups. Animals in each group receive one ofthe five following articles during the study:

-   -   1. Control vehicletopical    -   2. 0.25% Laquinimod topical    -   3. 1% Laquinimod topical    -   4. 4% Laquinimod topical    -   5. 0.1% Laquinimod oral

Topical Dosing:

Rats were dosed topically only on the surface of the left eye in whichOHT was induced. No article was administered on the un-operated righteye which served as the control.

The topical dose was administered on the surface of the left eye using acalibrated micro-pipette and a sterile tip. The volume for each topicaldose was 10 μL.

Rats were dosed twice daily, starting on the day of the first HSI untileuthanasia. The first daily dose was administered approximately between8 a.m. and 9 a.m. The second daily dose was administered approximatelybetween 4 p.m. and 5 p.m. On the day of euthanasia, rats were dosed onlyonce in the morning approximately between 8 a.m. and 9 a.m.

Oral Dosing:

Rats were dosed orally daily approximately between 8 a.m. and 10 a.m.,starting on the day of the first HSI until euthanasia. The last day ofdosing was the day of euthanasia. The volume for each oral dose was 1mL.

Post-Dose Procedures:

Chronic ocular hypertension (OHT) was created through two hypertonicsaline injections (HSI) which were performed one week apart in the lefteye. For each HSI, after the rats were anesthetized with a suitableanesthetic, a suture thread was passed through the left eyelid to fix itopen. A local anesthetic (e.g., 0.5% Proparacaine HCl OphthalmicSolution) was applied on the surgery eye topically. The conjunctiva wasincised with Vannas scissors to expose an episcleral vein. An occluderring with a groove was fitted around the left eye to provideunobstructed passage for the selected episcleral vein while obstructingthe other episcleral veins. Using a pulled-glass needle, 50-250 μL of1.8 M hypertonic saline solution was injected into the exposedepiscleral vein to scar the aqueous humor outflow pathway in an attemptto elevate IOP. The ring was removed shortly after the injection. Theun-operated right eye served as the control. Ophthalmic ointment wasapplied to both eyes to prevent corneal damage. For each HSI procedure,buprenorphine was administered subcutaneously for approximately 24 hoursto manage post-operative pains as appropriate. Clinical observations wasperformed at least once daily as described in Table 6.

Moribund and Dead Animals:

Animals were observed once daily for moribundity/mortality as part ofthe clinical observations. There were no moribound animals.

Measurements and Criterion:

IOP measurements were taken once weekly starting one week after thesecond HSI until euthanasia (a total of 5 measurements). Afterapplication of topical anesthesia (0.5% Proparacaine HCl OphthalmicSolution), IOP was measured on conscious rats on both eyes using aTono-Pen Vet tonometer (Reichert, Inc.; Depew, N.Y.). For eachtime-point, ten (10) IOP readings were recorded from each eye andaveraged. IOP measurements were taken around the same time (e.g.,between 10 a.m. and 2 p.m.) across measurement time-points to minimizethe circadian variability of IOP.

The IOP measurements were evaluated as follows: For each time-pointfollowing the HSI, the IOP elevation was calculated as the differencebetween the level in the left eye with OHT and that in the normal righteye (ΔIOP). The ΔIOP of the 5-weekly post-HSI IOP measurements wereaveraged and constitute the Mean ΔIOP for each animal. For each group,ten (10) animals with a sustained IOP elevation in the OHT eye wereselected from a larger pool and groups are matched for the Mean ΔIOP.Other animals were removed from the study and euthanized. Data wasanalyzed and reported for rats which did not have individual IOPmeasurements of ≧50 mmHg in the OHT eyes.

Ophthalmic Examinations:

Both eyes were examined and scored at one week after the second HSI andon the day of euthanasia, for a total of two times. Ophthalmicexaminations were performed according to the Classification System forGrading Ocular Lesions as described in Table 7, and the Ocular PosteriorSegment Scoring Scale of Table 8 using a hand-held slit-lamp and adirect ophthalmoscope or the surgical microscope. Posterior segmentexamination was performed after the topical application of Tropicamidein the conscious state, or after the rats are anesthetized withisoflorane inhalation.

Fluoro-Gold (FG) Back-Labeling of Retinal Ganglion Cells (RGC):

Approximately one week prior to euthanasia, RGC was labeled with theretrograde tracer FG. First, animals were sedated with appropriateanesthesia. Using a stereotaxic device, RGC was back-labeled with aninjection of 2.5 μL of 4% FG into the superior colliculus in eachhemisphere. Rats received subcutaneous injections of buprenorphine forapproximately 48 hours to manage post-surgery pain as appropriate.

Animals were euthanized by CO₂ inhalation 5-weeks after the 2^(nd) HSI.

Extraction and Processing of the Eyes and the Optic Nerves (ON):

The eyes were immediately enucleated with the optic nerve attached. Anapproximately 2.0 mm piece of the ON proximal to the globe is separatedand labeled with tissue mark to indicate the orientation of the nerve.The ON piece is placed in Modified Karnovsky's Fixative in 0.1 M Nacacodylate buffer and kept at 4±2° C. overnight. The next day ON piecewas washed at least three times for at least 10 minutes each in 0.1 M Nacacodylate buffer and stored in 0.1M Na cacodylate buffer at 4±2° C.After specimens were transferred to a contracted processing facility,within a week, the optic nerves were processed for plastic embedding:After post-fixation in 2% osmium tetroxide in 0.1 M Na cacodylate bufferfor at least 1.5 hours, ONs were dehydrated in graded ethanols,transitioned in propylene oxide and infiltrated with propylene oxide andepon mixtures. One to five (1-5) μm-thick cross-sections were taken viaa microtome at the ON end approximately 2.0 mm away from the globe. ONsections were stained with 1% toluidine blue and cover-slipped. Theprocessed specimens were returned. The identification of the ONs weremasked prior to injury analysis. The ON cross-sections were analyzed forinjury by light microscopy as follows:

The damaging effect of the sustained IOP elevation was assessed byqualitative microscopic analysis of the ON cross-sections using awell-established grading system described in Table 9. This methodallowed damage analysis of the entire retinal ganglion cell output (theON) in one section by light microscopy and was more sensitive thancounting total axons especially if there is mild nerve damage. SustainedIOP elevation resulted in degenerating, swollen axons and collapsedmyelin sheaths in the optic nerve. The extent of injury was then gradedby light microscopy based on a pattern of damage observed in rats withelevated IOP.

TABLE 9 Grading Scale for Optic Nerve Injury Grade 1 (Normal) Normaloptic nerve with healthy axons. Grade 2 (FOCAL INJURY) Degeneratingaxons with myelin debris are stained densely and appear focally. Someaxonal swellings are present. Grade 3 (INJURY SPREADING AWAY Severaldegenerating axons with myelin debris and axonal FROM FOCAL) swellingsspread away from the focal area. Normal axons still predominate. Grade 4(WIDE-SPREAD INJURY; Several degenerating axons with myelin debris andaxonal EQUIVALENT NUMBER of swellings are present throughout the nerve.There are DEGENERATING and NORMAL AXONS) approximately equal numbers ofnormal and abnormal axons. Grade 5 (WIDE-SPREAD INJURY; Degeneratingaxons with myelin debris and swollen axons DEGENERATING AXONS LARGELYlargely dominate the optic nerve, with gliosis in severe DOMINATE)cases.

The eyes were fixed in 4% paraformaldehyde (PFA) fixative at 4±2° C. forat least 24 hours. Retinas were dissected and flat whole-mounted forconfocal visualization and imaging. The actual identification of theretinal flat-mounts was masked prior to confocal imaging. Eight regionsper retina were imaged using a confocal microscope and the RGC in eachregion were counted as follows:

Retinal images were evaluated by confocal fluorescence microscopicexamination. A three-dimensional view of the x-axis, y-axis, and z-axiswere designed and processed using a specific system of image analysissoftware (Leica Confocal Software) to obtain an image of the viable RGCslabeled with FG. Two areas which were approximately 1.5 mm and 2.75 mmaway from the center of the ON head were selected in each retinalquadrant (8 regions per retina) and serial images of the retinalganglion cell layer were taken by the Confocal Microscope. Atwo-dimensional maximum projection image of the serial images was usedto count the viable RGCs using an image analysis software. The number ofviable RGCs per image was expressed in mm².

Evalution Criteria

The results of the study were considered in terms of the in-lifeobservations and any microscopic observations.

IOP Criterion:

For each time-point following the HSI, the IOP elevation was calculatedas the difference between the level in the left eye with OHT and that inthe normal right eye (ΔIOP). The ΔIOP of the 5-weekly post-HSI IOPmeasurements were averaged and constitute the Mean ΔIOP for each animal.For each group, ten (10) animals with a sustained IOP elevation in theOHT eye were selected from a larger pool and groups were matched for theMean ΔIOP. Other animals were removed from the study and euthanized.Data was analyzed and reported for rats which do not have individual IOPmeasurements of ≧50 mmHg in the OHT eyes.

Imaging of the Retinas by Confocal Microscopy:

Retinal images were evaluated by confocal fluorescence microscopicexamination. A three-dimensional view of the x-axis, y-axis, and z-axiswere designed and processed using a specific system of image analysissoftware (Leica Confocal Software) to obtain an image of the viable RGCslabeled with FG. Two areas which were approximately 1.5 mm and 2.75 mmaway from the center of the ON head were selected in each retinalquadrant (8 regions per retina) and serial images of the retinalganglion cell layer are taken by the Confocal Microscope. Atwo-dimensional maximum projection image of the serial images was usedto count the viable RGCs using an image analysis software. The number ofviable RGCs per image was expressed in mm².

Percent RGC loss in the OHT retinas was calculated in comparison to theRGC counts in the Non-OHT retina of the same animal using the followingformula: (100−(100×OHT/Non-OHT Mean RGC Counts per Retina)). The RGCcounts in each Non-OHT retina were considered 100% for that animal.

The damaging effect of the sustained IOP elevation was assessed byqualitative microscopic analysis of the ON cross-sections using awell-established grading system described in Table 9. This methodallowed damage analysis of the entire retinal ganglion cell output (theON) in one section by light microscopy and was more sensitive thancounting total axons especially if there is mild nerve damage. SustainedIOP elevation resulted in degenerating, swollen axons and collapsedmyelin sheaths in the optic nerve. The extent of injury was then gradedby light microscopy based on a pattern of damage observed in rats withelevated IOP.

Data Analysis:

Initially One-Way ANOVA was used to address statistically significantdifferences among groups. If there was a statistical significance, dataof the test groups was further compared with the data of the controlgroup using Dunnett's multiple comparison tests. Two-Way ANOVA, paired-t-tests, % neuroprotection calculations were also performed. Anydifferences between control and test animals was consideredstatistically significant only if the probability of the differencesbeing due to chance is equal to or less than 5% (p≦0.05; two-tailed).Statistical analysis is performed using Minitab, Minitab Inc, StatCollege, Pa. Any significant difference is further assessed forbiological relevance by comparison to the literature and historicaldata.

Results

TABLE 10 % RGC Loss (100 − (100 × OHT/Non-OHT Mean RGC Counts perRetina)) Route/ Laquinimod Mean % RGC Group Percentage Loss SD % RGCLoss 1 Topical/1% 17.6 33.8 2 Topical/ 34.8 42.7 Vehicle 3 Topical/4%26.8 36.4 4 Topical/0.25% 21.6 21.7 5 Oral/0.1% 22.9 33.1 RGC = RetinalGanglion Cell OHT = Ocular Hypertension SD = Standard Deviation

-   -   1. Per protocol, data were analyzed and reported for forty (40)        rats which did not have individual IOP measurements of ≧50 mmHg        in the OHT eyes.    -   2. Body Weights: The range of the baseline body weights of the        40 rats from Groups 1-5 was 258.6-351.3 grams at the start of        the study. On the day of dosing and the first HSI, body weight        range of all rats was 271.2-366.4 grams. A One-Way ANOVA        indicated that the group body weights were not statistically        different on the day of dosing (P=0.957). Rats weighed        271.4-349.3 grams on the day of euthanasia. Groups did not        differ in the amount of weight gained between the day of dosing        and the day of euthanasia (One-Way ANOVA; P=0.559).    -   3. Clinical Observations: There were no abnormal clinical        observations in the beginning of the study at the time of animal        assignment. Following the HSI surgeries, swelling of the surgery        eye, swelling of the conjunctiva and scleral/corneal        discoloration in the surgery eye were observed in all groups.        Following the Fluoro-Gold brain injection surgeries, hair loss        and skin wounds were noted in all groups due to the hair on the        skull being shaved prior to surgery and the skin on the skull        being incised and sutured after surgery. These observations were        expected and related with the glaucoma model creation (HSI) and        the Fluoro-gold brain injection surgeries. Abnormal clinical        observations which were not related with the HSI and FG        injection surgeries were hair loss in an animal from Group 2 and        in an animal from Group 5, and skin wound in 2 animals from        Group 5. Since Group 2 was the vehicle control group, these        abnormalities were incidental and not test-article related.    -   4. IOP Measurements (mmHg): None of the animals included in the        study had individual IOP measurements of ≧50 mmHg in the OHT        eyes. The Mean ΔIOP (OHT—Non-OHT) (Mean±SD) was 9.1±2.2 mmHg,        9.1±2.6 mmHg, 9.3±2.7 mmHg, 9.2±1.5 mmHg, and 9.1±2.9 mmHg for        Groups 1, 2, 3, 4 and 5, respectively. A One-Way ANOVA analysis        indicated that the groups were well-matched for Mean ΔIOP        (P>0.9) (FIG. 1). Representative images of the retinas with        FG-labeled RGC are shown in FIGS. 5A-5J. % FG—Labeled RGC loss        in the OHT retinas compared with the corresponding non-OHT        retinas is shown in Table 10. Compared to the non-OHT retinas, %        RGC Loss (Mean±SD) in the OHT retinas was 17.6±33.8, 34.8±42.7,        26.8±36.4, 21.6±21.7, and 22.9±33.1 for Groups 1, 2, 3, 4 and 5,        respectively (FIG. 2).    -   5. FG—labeled RGC counts: A Two-Way ANOVA on the RGC counts in        the OHT and Non-OHT (control) eyes versus groups did not show a        significant eye versus group interaction (P=0.919), indicating        that groups did not differ for the RGC counts in the OHT and        Non-OHT eyes (FIG. 3). As a secondary analysis, FG—Labeled RGC        counts per mm² were compared between the Non-OHT and the OHT        retinas for each group using a paired-t test (two-tailed). Group        2 (vehicle topical; P=0.047) and Group 4 (0.25% Laquinimod        topical; P=0.033) had fewer RGCs in the OHT eye compared to the        Non-OHT eyes. The number of RGCs in Group 3 (4% Laquinimod        topical; P=0.071) and Group 5 (0.1% Laquinimod oral; P=0.075)        were statistically marginally different between the OHT and        Non-OHT eyes. However, in Group 1 (1% Laquinimod topical), there        was no statistically significant difference in the RGC counts        between the OHT and Non-OHT eyes (P=0.189). This suggests that        the daily topical application of 1% Laquinimod may be        neuroprotective for the RGC.    -   6. Optic Nerve (ON) Injury Grades: Mean ON Injury Grades        (Mean±SD) for the Non-OHT eyes were 1.1±0.1, 1.2±0.2, 1.2±0.2,        1.2±0.3 and 1.2±0.2 for Groups 1, 2, 3, 4 and 5, respectively.        Mean Injury Grades (Mean±SD) for the OHT optic nerves were        2.5±1.3, 3.0±1.6, 3.0±1.5, 2.8±1.3 and 2.7±1.5 for Groups 1, 2,        3, 4, and 5, respectively. A Two-Way ANOVA on the Mean ON injury        grades in the OHT and Non-OHT (control) eyes versus groups did        not show a significant eye versus group interaction (P=0.98),        indicating that groups did not differ for the injury in the OHT        and Non-OHT optic nerves (FIG. 4). As a secondary analysis, Mean        ON Injury Grades were compared between the Non-OHT and the OHT        optic nerves for each group using two-tailed paired-t tests. The        Mean ON injury grades were significantly greater in the OHT eyes        compared to the Non-OHT control eyes in all groups (P<0.05).    -   7. Ophthalmic Examinations (OEs): At baseline ocular        examinations prior to initial dose, there were no ocular        abnormalities observed in either eye in any of the animals        included in the study. During the post-dose OEs, there were no        ocular problems observed in any of the animals in the Non-OHT        eyes. However, there were some ocular abnormalities observed in        the OHT eyes due to the glaucoma-model creation procedures        (hypertonic saline injection surgeries into the episcleral        veins) in all groups. These abnormalities included minor        congestion and chemosis (swelling) in the conjunctiva, minor        corneal opacities, lack of sufficient dilation of the pupil        after application of the pupil-dilating agent Tropicamide,        slight opacities in the lens and presence of free-floating iris        pigments in front of the lens in the OHT eyes. The post-HSI        ocular findings in the OHT eyes were observed in all groups with        a similar occurrence and were not test articlerelated.

Conclusion

The study involved daily dosing of five groups for approximately sixweeks: Group 1 (1% Laquinimod topical), Group 2 (Vehicle topical), Group3 (4% Laquinimod topical), Group 4 (0.25% Laquinimod topical) and Group5 (0.1% Laquinimod oral). The analyses for the RGC counts in Group 1animals suggested a trend towards neuroprotection following dailytopical application of 1% Laquinimod.

EXAMPLE 2 Assessment of Efficacy of Laquinimod for Treating PatientsAfflicted with Glaucoma

Periodic (e.g., daily or twice daily) administration of laquinimod (oralor topical) is effective in treating glaucoma human patients. Periodic(e.g., daily or twice daily) administration of laquinimod (oral ortopical) is effective to reduce a glaucoma-associated symptom in thesubject.

A laquinimod composition as described herein is administeredsystematically or locally to the eye of a subject suffering fromglaucoma. The administration of the composition is effective to treatthe subject suffering from glaucoma. The administration of thecomposition is also effective to reduce a glaucoma-associated symptom ofglaucoma in the subject. The administration of the composition is alsoeffective to reduce intraocular pressure in the subject. Theadministration of the composition is effective to reduce RGC damageand/or RGC loss, and improve RGC viability in the subject.

REFERENCES

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What is claimed is:
 1. A method of treating a subject afflicted withglaucoma comprising administering to the subject an amount of laquinimodeffective to treat the subject.
 2. The method of claim 1, wherein theadministration of laquinimod is effective to reduce or inhibit a symptomof the glaucoma in the subject.
 3. The method of claim 2, wherein thesymptom is retinal ganglion cell damage, retinal ganglion cell loss, orelevated intraocular pressure.
 4. The method of any one of claims 1-3,wherein laquinimod is laquinimod sodium.
 5. The method of any one ofclaims 1-4, wherein the route of administration of laquinimod isintraocular, periocular, ocular, oral, systemic or topical.
 6. Themethod of any one of claims 1-5, wherein laquinimod is administered inthe form of an aerosol, an inhalable powder, an injectable, a liquid, agel, a solid, a capsule or a tablet.
 7. The method of claim 6, whereinthe concentration of laquinimod in the liquid or gel is 5-100 mg/mlsolution, 20-100 mg/ml solution, 10-15 mg/ml solution, or 20-50 mg/mlsolution.
 8. The method of any one of claims 1-7, wherein laquinimod isadministered periodically.
 9. The method of claim 8, wherein laquinimodis administered daily.
 10. The method of claim 8, wherein laquinimod isadministered more often than once daily or less often than once daily.11. The method of any one of claims 1-10, wherein the amount laquinimodadministered is at least 0.2 mg/day and/or less than 0.6 mg/day.
 12. Themethod of any one of claims 1-10, wherein the amount laquinimodadministered is 0.03-600 mg/day, 0.1-40.0 mg/day, 0.1-2.5 mg/day,0.25-2.0 mg/day, 0.5-1.2 mg/day, 0.25 mg/day, 0.3 mg/day, 0.5 mg/day,0.6 mg/day, 1.0 mg/day, 1.2 mg/day, 1.5 mg/day or 2.0 mg/day.
 13. Themethod of any one of claims 1-12, wherein the amount of laquinimodadministered is 0.05-4.0 mg per administration, 0.05-2.0 mg peradministration, 0.2-4.0 mg per administration, 0.2-2.0 mg peradministration, about 0.1 mg per administration, or about 0.5 mg peradministration.
 14. The method of any one of claims 1-13, furthercomprising administration of a second agent for the treatment ofglaucoma.
 15. The method of claim 14, wherein the second agent is aβ-adrenergic antagonist, adrenergic agonist, parasympathomimetic,prostaglandin-like analog, or carbonic anhydrase inhibitor.
 16. Themethod of any one of claims 8-15, wherein the periodic administration oflaquinimod continues for at least 3 days, more than 30 days, more than42 days, 8 weeks or more, at least 12 weeks, at least 24 weeks, morethan 24 weeks, or 6 months or more.
 17. The method of any one of claims1-16, wherein the subject is a human patient.
 18. A method of treating asubject suffering from retinal ganglion cell loss or retinal ganglioncell damage, or of reducing retinal ganglion cell loss or damage in asubject, comprising administering to the subject an amount of laquinimodeffective to reduce retinal ganglion cell loss or retinal ganglion celldamage in the subject.
 19. A method of treating a subject suffering fromelevated intraocular pressure, or of reducing intraocular pressure in asubject, comprising administering to the subject an amount of laquinimodeffective to reduce intraocular pressure in the subject.
 20. A packagecomprising: a) a pharmaceutical composition comprising an amount oflaquinimod; and b) instruction for use of the pharmaceutical compositionto treat a subject afflicted with glaucoma.
 21. The package of claim 20,wherein the package comprises a second pharmaceutical compositioncomprising an amount of a second agent for the treatment of glaucoma.22. The package of claim 21, wherein the second agent is a β-adrenergicantagonist, adrenergic agonist, parasympathomimetic, prostaglandin-likeanalog, or carbonic anhydrase inhibitor.
 23. The package of any one ofclaims 20-22, wherein the pharmaceutical composition is the form of anaerosol, an inhalable powder, an injectable, a liquid, a gel, a solid, acapsule or a tablet.
 24. The package of claim 23, wherein theconcentration of laquinimod in the liquid or gel is 5-100 mg/mlsolution, 20-100 mg/ml solution, 10-15 mg/ml solution or 20-50 mg/mlsolution.
 25. The package of claim 23, wherein the tablets are coatedwith a coating which inhibits oxygen from contacting the core.
 26. Thepackage of claim 25, wherein the coating comprises a cellulosic polymer,a detackifier, a gloss enhancer, or pigment.
 27. The package of any oneof claims 20-26, wherein the pharmaceutical composition furthercomprises mannitol, an alkalinizing agent, an oxidation reducing agent,a lubricant, a filler, and/or a desiccant.
 28. The package of claim 27,wherein the alkalinizing agent is meglumine.
 29. The package of any oneof claims 20-27, wherein the pharmaceutical composition is stable andfree of an alkalinizing agent or an oxidation reducing agent, preferablythe pharmaceutical composition is free of an alkalinizing agent and freeof an oxidation reducing agent.
 30. The package of any one of claims20-29, wherein the pharmaceutical composition is stable and free ofdisintegrant.
 31. The package of claim 27, wherein the lubricant ispresent in the pharmaceutical composition as solid particles.
 32. Thepackage of claims 27 or 31, wherein the lubricant is sodium stearylfumarate or magnesium stearate.
 33. The package of claim 27, wherein thefiller is present in the pharmaceutical composition as solid particles.34. The package of claims 27 or 33, wherein the filler is lactose,lactose monohydrate, starch, isomalt, mannitol, sodium starch glycolate,sorbitol, lactose spray dried, lactose anhydrouse, or a combinationthereof.
 35. The package of claim 27, wherein the desiccant is silicagel.
 36. The package of any one of claims 20-35, wherein thepharmaceutical composition is stable and has a moisture content of nomore than 4%.
 37. The package of any one of claims 20-36, whereinlaquinimod is present in the pharmaceutical composition as solidparticles.
 38. The package of any one of claims 20-37, wherein thepackage is a sealed packaging having a moisture permeability of not morethan 15 mg/day per liter or a blister pack having a maximum moisturepermeability of not more than 0.005 mg/day.
 39. The package of claim 38,wherein the sealed package is a bottle or comprises an HDPE bottle,preferably the bottle is closed with a heat induction liner.
 40. Thepackage of claims 38 or 39, wherein the sealed package comprises anoxygen absorbing agent, which oxygen absorbing agent is preferably iron.41. The package of any one of claims 20-40, wherein the amount oflaquinimod in the pharmaceutical composition is at least 0.2 mg, lessthan 0.6 mg, 0.1-40.0 mg, 0.03-600 mg, 0.1-2.5 mg, 0.25-2.0 mg, 0.5-1.2mg, 0.25 mg, 0.3 mg, 0.5 mg, 0.6 mg, 1.0 mg, 1.2 mg, 1.5 mg, or 2.0 mg.42. The package of any one of claims 20-41, wherein the pharmaceuticalcomposition comprises unit doses of laquinimod of 0.05-4.0 mg, 0.05-2.0mg, 0.2-4.0 mg, 0.2-2.0 mg, about 0.1 mg, or about 0.5 mg.
 43. Thepackage of any one of claims 20-42, wherein the pharmaceuticalcomposition is formulated for intraocular, periocular, ocular, oral,systemic or topical administration.
 44. The package of any one of claims20-43, for use in treating a subject afflicted with glaucoma.
 45. Atherapeutic package for dispensing to, or for use in dispensing to, asubject afflicted with glaucoma, which comprises: a) one or more unitdoses, each such unit dose comprising an amount of laquinimod thereof,wherein the amount of said laquinimod in said unit dose is effective,upon administration to said subject, to treat the subject, and b) afinished pharmaceutical container therefor, said container containingsaid unit dose or unit doses, said container further containing orcomprising labeling directing the use of said package in the treatmentof said subject.
 46. The therapeutic package of claim 45, wherein thepackage comprises a second pharmaceutical composition comprising anamount of a second agent for the treatment of glaucoma.
 47. Thetherapeutic package of claim 46, wherein the second agent is aβ-adrenergic antagonist, adrenergic agonist, parasympathomimetic,prostaglandin-like analog, or carbonic anhydrase inhibitor.
 48. Apharmaceutical composition comprising an amount of laquinimod for use intreating a subject afflicted glaucoma.
 49. The pharmaceuticalcomposition of claim 48, comprising an amount of a second agent for thetreatment of glaucoma.
 50. The pharmaceutical composition of claim 49,wherein the second agent is a β-adrenergic antagonist, adrenergicagonist, parasympathomimetic, prostaglandin-like analog, or carbonicanhydrase inhibitor.
 51. The pharmaceutical composition of any one ofclaims 48-50, in the form of an aerosol, an inhalable powder, aninjectable, a liquid, a gel, a solid, a capsule or a tablet.
 52. Thepharmaceutical composition of claim 51, wherein the concentration oflaquinimod in the liquid or gel is 5-100 mg/ml solution, 20-100 mg/mlsolution, 10-15 mg/ml solution or 20-50 mg/ml solution.
 53. Thepharmaceutical composition of claim 51, comprising a unit dose of 10pLof an aqueous pharmaceutical solution which contains in solution atleast 0.2 mg laquinimod.
 54. The pharmaceutical composition of any oneof claims 48-53, wherein laquinimod is laquinimod sodium.
 55. Thepharmaceutical composition of claim 51, wherein the tablets are coatedwith a coating which inhibits oxygen from contacting the core.
 56. Thepharmaceutical composition of claim 55, wherein the coating comprises acellulosic polymer, a detackifier, a gloss enhancer, or pigment.
 57. Thepharmaceutical composition of any one of claims 48-56, furthercomprising mannitol, an alkalinizing agent, an oxidation reducing agent,a lubricant and/or a filler.
 58. The pharmaceutical composition of claim57, wherein the alkalinizing agent is meglumine.
 59. The pharmaceuticalcomposition of any one of claims 48-57, which is free of an alkalinizingagent or an oxidation reducing agent, preferably the pharmaceuticalcomposition is free of an alkalinizing agent and free of an oxidationreducing agent.
 60. The pharmaceutical composition of any one of claims48-59, which is stable and free of disintegrant.
 61. The pharmaceuticalcomposition of claim 57, wherein the lubricant is present in thepharmaceutical composition as solid particles.
 62. The pharmaceuticalcomposition of claims 57 or 61, wherein the lubricant is sodium stearylfumarate or magnesium stearate.
 63. The pharmaceutical composition ofclaim 57, wherein the filler is present in the pharmaceuticalcomposition as solid particles.
 64. The pharmaceutical composition ofclaims 57 or 63, wherein the filler is lactose, lactose monohydrate,starch, isomalt, mannitol, sodium starch glycolate, sorbitol, lactosespray dried, lactose anhydrouse, or a combination thereof.
 65. Thepharmaceutical composition of any one of claims 48-64, wherein theamount of laquinimod is at least 0.2 mg, less than 0.6 mg, 0.1-40.0 mg,0.03-600 mg, 0.1-2.5 mg, 0.25-2.0 mg, 0.5-1.2 mg, 0.25 mg, 0.3 mg, 0.5mg, 0.6 mg, 1.0 mg, 1.2 mg, 1.5 mg, or 2.0 mg.
 66. The pharmaceuticalcomposition of any one of claims 48-65, comprising unit doses oflaquinimod of 0.05-4.0 mg, 0.05-2.0 mg, 0.2-4.0 mg, 0.2-2.0 mg, about0.1 mg, or about 0.5 mg.
 67. The pharmaceutical composition of any oneof claims 48-66, formulated for intraocular, periocular, ocular, oral,systemic or topical administration.
 68. The pharmaceutical compositionof any one of claims 48-67, for use in treating a subject afflicted withglaucoma.
 69. A pharmaceutical composition in unit dosage form, usefulin treating a subject afflicted with glaucoma, which comprises an amountof laquinimod; which amount of said laquinimod in said composition iseffective, upon administration to said subject of one or more of saidunit dosage forms of said composition, to treat the subject.
 70. Apackage comprising: a) a pharmaceutical composition of any one of claims48-69; and b) instruction for use of the pharmaceutical composition totreat a subject afflicted with glaucoma.
 71. Laquinimod for themanufacture of a medicament for use in treating a subject afflictedglaucoma.